Primary Prevention of Sudden Cardiac Death With Implantable Cardioverter-Defibrillator Therapy in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 05 11 2018
revised: 19 12 2018
accepted: 20 12 2018
pubmed: 27 1 2019
medline: 10 1 2020
entrez: 26 1 2019
Statut: ppublish

Résumé

Implantable cardioverter-defibrillator (ICD) therapy remains a corner stone of sudden cardiac death (SCD) prevention in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC). We aimed to assess predictors of appropriate ICD therapies in the Scandinavian cohort of ARVC patients who received ICD for primary prevention of SCD. Study group comprised of 79 definite ARVC patients by 2010 Task Force criteria (60% male, age at ICD implant 39 ± 14 years) who were enrolled in the Nordic ARVC Registry and received an ICD for primary SCD prevention. The primary end point of appropriate ICD shock or death from any cause was assessed and compared with 137 definite ARVC patients who received ICD for secondary SCD prevention (74% male, age at ICD implant 42 ± 15 years). In the study group, 38% were ≤35 years of age at baseline, 25% had nonsustained ventricular tachycardia, and 29% had syncope at baseline. Major repolarization abnormality (hazard ratio = 4.00, 95% confidence interval 1.30 to 12.30, p = 0.015) and age ≤35 years (hazard ratio = 4.21, 95% confidence interval 1.49 to 11.85, p = 0.001) independently predicted the primary end point. The outcome did not differ between the primary prevention patients with either of these risk factors and the secondary prevention cohort (2% to 4% annual event rate) whereas patients without risk factors did not have any appropriate ICD shocks during follow-up. In conclusion, young age at ARVC diagnosis and major repolarization abnormality independently predict ICD shocks or death in the primary prevention ICD recipients and associated with the event rate similar to the one observed in the secondary prevention cohort. Our data indicate the benefit of ICD for primary prevention in patients with any of these risk factors.

Identifiants

pubmed: 30678832
pii: S0002-9149(19)30056-6
doi: 10.1016/j.amjcard.2018.12.049
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1156-1162

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Pyotr G Platonov (PG)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden. Electronic address: pyotr.platonov@gmail.com.

Kristina H Haugaa (KH)

Center for Cardiological Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Henning Bundgaard (H)

Department of Cardiology, The Heart Center, Rigshospitalet, University of Copenhagen, Denmark & Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Anneli Svensson (A)

Department of Cardiology and Department of Medical and Health Sciences, Linköping University, Linköping, Sweden.

Thomas Gilljam (T)

Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Jim Hansen (J)

Department of Cardiology, Herlev-Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.

Trine Madsen (T)

Department of Cardiology, Aalborg University Hospital, Aalborg, Denmark.

Anders Gaarsdal Holst (AG)

Department of Cardiology, The Heart Center, Rigshospitalet, University of Copenhagen, Denmark & Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Jonas Carlson (J)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.

Øyvind H Lie (ØH)

Center for Cardiological Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Morten Kvistholm Jensen (M)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Thor Edvardsen (T)

Center for Cardiological Innovation, Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway; Institute for Clinical Medicine, University of Oslo, Oslo, Norway.

Henrik K Jensen (HK)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Health, Aarhus University, Denmark.

Jesper H Svendsen (JH)

Department of Cardiology, The Heart Center, Rigshospitalet, University of Copenhagen, Denmark & Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

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